rs3732378, CX3CR1

N. diseases: 48
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Acquired Immunodeficiency Syndrome
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
42 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2005 2005
Acute otitis media
CUI: C0271429
Disease: Acute otitis media
1 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2018 2018
Anthracosis
CUI: C0003165
Disease: Anthracosis
37 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
Cardiovascular Abnormalities
CUI: C0243050
Disease: Cardiovascular Abnormalities
12 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2003 2003
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1 2009 2009
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2005 2005
Chronic tonsillitis
CUI: C0149517
Disease: Chronic tonsillitis
3 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2007 2007
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2016 2016
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2011 2011
Endothelial dysfunction
CUI: C0856169
Disease: Endothelial dysfunction
25 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2009 2009
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2008 2008
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2016 2016
Infectious Otitis Media
CUI: C2827407
Disease: Infectious Otitis Media
6 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
1111 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2014 2014
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2012 2012
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1 2003 2003
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2013 2013